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FDA 510(k), K953337, BETA HIP PROSTHESIS
FDA 510(k), K953337, BETA HIP PROSTHESIS
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510(K) Number: K953337
Device Name: BETA HIP PROSTHESIS
Manufacturer: ZIMMER, INC.
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 07/17/1995
Decision Date: 01/22/1996
Regulation Medical Specialty: Orthopedic
Device Name: BETA HIP PROSTHESIS
Manufacturer: ZIMMER, INC.
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 07/17/1995
Decision Date: 01/22/1996
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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